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American Journal of Human Genetics|June 1, 1990
The children of parents exposed to atomic bombs: estimates of the genetic doubling dose of radiation for humansJ V Neel, W J Schull, A A Awa, et al.American Journal of Human Genetics|June 1, 1990
The frequency of aneuploidy in cultured lymphocytes is correlated with age and gender but not with reproductive historyG P Nowinski, D L Van Dyke, B C Tilley, et al.American Journal of Human Genetics|June 1, 1990
Exclusion of linkage between the human apolipoprotein B gene and abetalipoproteinemiaL S Huang, P A Jänne, J de Graaf, et al.American Journal of Human Genetics|March 5, 2013
Constitutional mutations in RTEL1 cause severe dyskeratosis congenitaAmanda J Walne, Tom Vulliamy, Michael Kirwan, et al.American Journal of Human Genetics|March 5, 2013
Mutations in c12orf57 cause a syndromic form of colobomatous microphthalmiaFatema Zahrani, Mohammed A Aldahmesh, Muneera J Alshammari, et al.American Journal of Human Genetics|March 5, 2013
Whole-exome sequencing identifies mutated c12orf57 in recessive corpus callosum hypoplasiaNaiara Akizu, Nuri M Shembesh, Tawfeg Ben-Omran, et al.American Journal of Human Genetics|February 21, 2012
Revertant somatic mosaicism by mitotic recombination in dyskeratosis congenitaMarjolijn C J Jongmans, Eugene T P Verwiel, Yvonne Heijdra, et al.American Journal of Human Genetics|February 21, 2012
Mutations in LOXHD1, a recessive-deafness locus, cause dominant late-onset Fuchs corneal dystrophyS Amer Riazuddin, David S Parker, Elyse J McGlumphy, et al.American Journal of Human Genetics|April 2, 2013
Complete haplotype sequence of the human immunoglobulin heavy-chain variable, diversity, and joining genes and characterization of allelic and copy-number variationCorey T Watson, Karyn M Steinberg, John Huddleston, et al.American Journal of Human Genetics|April 23, 2013
Mutations in ANTXR1 cause GAPO syndromeViktor Stránecký, Alexander Hoischen, Hana Hartmannová, et al.Pageof 980